TY - JOUR
T1 - Tpl2/Cot signals activate ERK, JNK, and NF-kappa B in a cell-type and stimulus-specific manner
AU - Das, S
AU - Cho, J
AU - Lambertz, I
AU - Kelliher, MA
AU - Eliopoulos, Aristides
AU - Du, KY
AU - Tsichlis, PN
PY - 2005/6/1
Y1 - 2005/6/1
N2 - Macrophages and B-cells from Tpl2 knock-out mice exhibit a restricted defect in lipopolysaccharide and death receptor signaling that is limited to the activation of ERK. Here we show that Tpl2(-/-) MEFs exhibit defects in ERK, JNK, and NF-kappa B activation, or ERK activation only when stimulated with tumor necrosis factor-alpha (TNF-alpha) or interleukin-1 beta, respectively. In addition, we show that the activation of Tpl2 by TNF-alpha depends on signals transduced by both TRAF2 and RIP1. Activated Tpl2 phosphorylates MKK4/SEK1 upstream of JNK and stimulates NF-kappa B DNA binding and transcriptional activity by mechanisms that are independent of the nuclear translocation of p50 and p65. Tpl2-transduced TNF-alpha signals instead promote the phosphorylation of p65 at Ser(276) and modulate the spectrum of proteins associated with p65. Phosphorylation stimulates the transcriptional activity of NF-kappa B but does not affect its ability to bind DNA, which may be affected by the composition of the nuclear NF-kappa B complexes. These data confirm that defects caused by a single mutation may be cell-type and signal-specific and delineate the role of Tpl2 in the transduction of TNF-alpha signals that activate JNK and NF-kappa B in MEFs.
AB - Macrophages and B-cells from Tpl2 knock-out mice exhibit a restricted defect in lipopolysaccharide and death receptor signaling that is limited to the activation of ERK. Here we show that Tpl2(-/-) MEFs exhibit defects in ERK, JNK, and NF-kappa B activation, or ERK activation only when stimulated with tumor necrosis factor-alpha (TNF-alpha) or interleukin-1 beta, respectively. In addition, we show that the activation of Tpl2 by TNF-alpha depends on signals transduced by both TRAF2 and RIP1. Activated Tpl2 phosphorylates MKK4/SEK1 upstream of JNK and stimulates NF-kappa B DNA binding and transcriptional activity by mechanisms that are independent of the nuclear translocation of p50 and p65. Tpl2-transduced TNF-alpha signals instead promote the phosphorylation of p65 at Ser(276) and modulate the spectrum of proteins associated with p65. Phosphorylation stimulates the transcriptional activity of NF-kappa B but does not affect its ability to bind DNA, which may be affected by the composition of the nuclear NF-kappa B complexes. These data confirm that defects caused by a single mutation may be cell-type and signal-specific and delineate the role of Tpl2 in the transduction of TNF-alpha signals that activate JNK and NF-kappa B in MEFs.
U2 - 10.1074/jbc.M412837200
DO - 10.1074/jbc.M412837200
M3 - Article
C2 - 15833743
SN - 1083-351X
VL - 280
SP - 23748
EP - 23757
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 25
ER -